Canonical Allele Identifier: CA2047190481
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004919_76004924delinsCCTGTA , CM000674.2:g.76004919_76004924delinsCCTGTA GRCh38
NC_000012.11:g.76398699_76398704delinsCCTGTA , CM000674.1:g.76398699_76398704delinsCCTGTA GRCh37
NC_000012.10:g.74684966_74684971delinsCCTGTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1265_311+1270delinsTACAGG
XR_001749218.2:n.402+1265_402+1270delinsTACAGG
XR_945110.3:n.402+1265_402+1270delinsTACAGG